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Vascular parkinsonism in a CADASIL case with an intact nigrostriatal dopaminergic system.

作者信息

Wegner F, Strecker K, Schwarz J, Wagner A, Heinritz W, Sommerer F, Thal D R, Schneider J-P, Kendziorra K, Sabri O

出版信息

J Neurol. 2007 Dec;254(12):1743-5. doi: 10.1007/s00415-007-0529-4. Epub 2007 Nov 21.

DOI:10.1007/s00415-007-0529-4
PMID:18004646
Abstract
摘要

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Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies.经活检证实的伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的突变谱:对诊断策略的影响
Arch Neurol. 2005 Jul;62(7):1091-4. doi: 10.1001/archneur.62.7.1091.
2
Cerebral small vessel diseases: cerebral microangiopathies.脑小血管病:脑微血管病变
Curr Opin Neurol. 2005 Apr;18(2):179-88. doi: 10.1097/01.wco.0000162861.26971.03.
3
Vascular parkinsonism--an important cause of parkinsonism in older people.血管性帕金森综合征——老年人帕金森综合征的一个重要病因。
病例报告:无痴呆的伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病继发进行性不对称帕金森病
Front Neurol. 2022 Jan 10;12:760164. doi: 10.3389/fneur.2021.760164. eCollection 2021.
4
Vascular parkinsonism--characteristics, pathogenesis and treatment.血管性帕金森综合征——特征、发病机制与治疗。
Nat Rev Neurol. 2015 Jun;11(6):319-26. doi: 10.1038/nrneurol.2015.61. Epub 2015 Apr 28.
5
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.遗传性弥漫性脑白质病伴腔隙(HDLS)和 CSF1R 突变患者的帕金森特征。
Parkinsonism Relat Disord. 2013 Oct;19(10):869-77. doi: 10.1016/j.parkreldis.2013.05.013. Epub 2013 Jun 17.
6
First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family.NOTCH3 基因exon 24 致病性突变在 CADASIL 家族中的首次报道。
J Neurol. 2011 Sep;258(9):1632-6. doi: 10.1007/s00415-011-5983-3. Epub 2011 Mar 16.
Age Ageing. 2005 Mar;34(2):114-9. doi: 10.1093/ageing/afi025.
4
Combined 123I-FP-CIT and 123I-IBZM SPECT for the diagnosis of parkinsonian syndromes: study on 72 patients.联合使用123I-FP-CIT和123I-IBZM单光子发射计算机断层扫描(SPECT)诊断帕金森综合征:72例患者的研究
J Neural Transm (Vienna). 2005 May;112(5):677-92. doi: 10.1007/s00702-004-0208-x. Epub 2004 Sep 14.
5
Basal ganglia involvement of a patient with SCA 17--a new form of autosomal dominant spinocerebellar ataxia.一名患有SCA 17(常染色体显性遗传性脊髓小脑共济失调的一种新形式)患者的基底神经节受累情况
J Neurol. 2004 Jul;251(7):896-7. doi: 10.1007/s00415-004-0462-8.
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Progressive supranuclear palsy phenotype secondary to CADASIL.伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病继发的进行性核上性麻痹表型
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Diagnostic strategies in CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的诊断策略
Neurology. 2002 Oct 22;59(8):1134-8. doi: 10.1212/wnl.59.8.1134.
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[123I]beta-CIT SPECT distinguishes vascular parkinsonism from Parkinson's disease.[123I]β-CIT单光子发射计算机断层扫描可区分血管性帕金森综合征与帕金森病。
Mov Disord. 2002 May;17(3):518-23. doi: 10.1002/mds.10092.
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The phenotypic spectrum of CADASIL: clinical findings in 102 cases.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的表型谱:102例临床发现
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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病中的全身血管平滑肌细胞损伤
Acta Neuropathol. 1995;89(6):500-12. doi: 10.1007/BF00571504.